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Cited by 369

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Atomic Metal–Support Interaction Enables Reconstruction-Free Dual-Site Electrocatalyst

Sun, Huachuan, Tung, Ching-Wei, Qiu, Yang, Zhang, Wei, Wang, Qi, Li, Zhishan, Tang, Jiang, Chen, Hsiao-Chien, Wang, Chundong, Chen, Hao Ming·2022·Journal of the American Chemical Society

Abstract

Real bifunctional electrocatalysts for hydrogen evolution reaction and oxygen evolution reaction have to be the ones that exhibit a steady configuration during/after reaction without irreversible structural transformation or surface reconstruction. Otherwise, they can be termed as “precatalysts” rather than real catalysts. Herein, through a strongly atomic metal–support interaction, single-atom dispersed catalysts decorating atomically dispersed Ru onto a nickel–vanadium layered double hydroxide (LDH) scaffold can exhibit excellent HER and OER activities. Both in situ X-ray absorption spectroscopy and operando Raman spectroscopic investigation clarify that the presence of atomic Ru on the surface of nickel–vanadium LDH is playing an imperative role in stabilizing the dangling bond-rich surface and further leads to a reconstruction-free surface. Through strong metal–support interaction provided by nickel–vanadium LDH, the significant interplay can stabilize the reactive atomic Ru site to reach a small fluctuation in oxidation state toward cathodic HER without reconstruction, while the atomic Ru site can stabilize the Ni site to have a greater structural tolerance toward both the bond constriction and structural distortion caused by oxidizing the Ni site during anodic OER and boost the oxidation state increase in the Ni site that contributes to its superior OER performance. Unlike numerous bifunctional catalysts that have suffered from the structural reconstruction/transformation for adapting the HER/OER cycles, the proposed Ru/Ni 3 V-LDH is characteristic of steady dual reactive sites with the presence of a strong metal–support interaction (i.e., Ru and Ni sites) for individual catalysis in water splitting and is revealed to be termed as a real bifunctional electrocatalyst.

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Metadata

Authors
Sun, H., Tung, C.-W., Qiu, Y., Zhang, W., Wang, Q., Li, Z., Tang, J., Chen, H.-C., Wang, C., & Chen, H. M.
Venue
Journal of the American Chemical Society
Published
2021-12-22
Volume
144
Issue
3
Pages
1174-1186
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W4200317775
Cited by
369
References
57
FWCI
11.71
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Atomic Metal–Support Interaction Enables Reconstruction-Free Dual-Site Electrocatalyst. https://app.cochat.ai/papers/10.1021/jacs.1c08890
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Sun, H., Tung, C.-W., Qiu, Y., Zhang, W., Wang, Q., Li, Z., Tang, J., Chen, H.-C., Wang, C., & Chen, H. M. (2022). Atomic Metal–Support Interaction Enables Reconstruction-Free Dual-Site Electrocatalyst. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.1c08890

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